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Regina Waltes

Showing results (11-20 of 21) with videos related to

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Translational Psychiatry|July 7, 2020
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorderAfsheen Yousaf, Regina Waltes, Denise Haslinger, et al.
Plos One|January 28, 2022
The methylome in females with adolescent Conduct Disorder: Neural pathomechanisms and environmental risk factorsAndreas G Chiocchetti, Afsheen Yousaf, Regina Waltes, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 18, 2017
Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilitiesAndreas G Chiocchetti, Afsheen Yousaf, Hannah S Bour, et al.
Epilepsia|July 24, 2025
The transcriptomic signature of DEPDC5 KO induced mTOR hyperactivation in human neurons and its response to rapamycin treatmentMattson S O Jones, Silvia Lindlar, Johannes Ludwig, et al.
The Journal of Biological Chemistry|July 16, 2011
ATM protein-dependent phosphorylation of Rad50 protein regulates DNA repair and cell cycle controlMagtouf Gatei, Burkhard Jakob, Philip Chen, et al.
Molecular Autism|November 17, 2018
Loss of the Chr16p11.2 ASD candidate gene <i>QPRT</i> leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell modelDenise Haslinger, Regina Waltes, Afsheen Yousaf, et al.
Human Genetics|January 21, 2014
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disordersRegina Waltes, Eftichia Duketis, Michael Knapp, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 10, 2010
Missense variants in ATM in 26,101 breast cancer cases and 29,842 controlsOlivia Fletcher, Nichola Johnson, Isabel dos Santos Silva, et al.
Genome Medicine|May 18, 2022
Breast cancer risks associated with missense variants in breast cancer susceptibility genesLeila Dorling, Sara Carvalho, Jamie Allen, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Translational Psychiatry|July 7, 2020
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorderAfsheen Yousaf, Regina Waltes, Denise Haslinger, et al.
Plos One|January 28, 2022
The methylome in females with adolescent Conduct Disorder: Neural pathomechanisms and environmental risk factorsAndreas G Chiocchetti, Afsheen Yousaf, Regina Waltes, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 18, 2017
Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilitiesAndreas G Chiocchetti, Afsheen Yousaf, Hannah S Bour, et al.
Epilepsia|July 24, 2025
The transcriptomic signature of DEPDC5 KO induced mTOR hyperactivation in human neurons and its response to rapamycin treatmentMattson S O Jones, Silvia Lindlar, Johannes Ludwig, et al.
The Journal of Biological Chemistry|July 16, 2011
ATM protein-dependent phosphorylation of Rad50 protein regulates DNA repair and cell cycle controlMagtouf Gatei, Burkhard Jakob, Philip Chen, et al.
Molecular Autism|November 17, 2018
Loss of the Chr16p11.2 ASD candidate gene <i>QPRT</i> leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell modelDenise Haslinger, Regina Waltes, Afsheen Yousaf, et al.
Human Genetics|January 21, 2014
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disordersRegina Waltes, Eftichia Duketis, Michael Knapp, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 10, 2010
Missense variants in ATM in 26,101 breast cancer cases and 29,842 controlsOlivia Fletcher, Nichola Johnson, Isabel dos Santos Silva, et al.
Genome Medicine|May 18, 2022
Breast cancer risks associated with missense variants in breast cancer susceptibility genesLeila Dorling, Sara Carvalho, Jamie Allen, et al.
Pageof 3